Gene Name |
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 |
actin-like 6A |
Image |
|
No pdb structure |
Gene Ontology Annotations |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
- Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) ( 23453885)
|
|
Protein-Protein Interactions |
26 interactors:
ACTL6A
ACTL6B
AR
ARID1B
BEND7
BRCA1
CEBPA
DPF3
ESR1
HIST1H3A
KHDRBS1
MDM2
MDM4
MECP2
MYB
MYC
NR0B2
NR3C1
NR4A2
PHB
PITX1
PRMT5
PRPF6
SDCBP
SIN3B
SS18
|
13 interactors:
ARHGDIA
CDK2
CDK9
EWSR1
FLII
MRGBP
MYC
POLR2A
RELA
RUVBL1
SMARCA2
SMARCA4
TRRAP
|
Entrez ID |
6595 |
86 |
HPRD ID |
02483 |
05389 |
Ensembl ID |
ENSG00000080503
|
ENSG00000136518
|
Uniprot IDs |
P51531
Q56A76
Q8N9Q1
|
O96019
|
PDB IDs |
2DAT
|
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
abnormality
arid1a
coinactivation
copyright
fish
frame
harboring
heterozygous
infancy
insights
malignancies
missense
monoploid
mrts
pbrm1
protected
remodeling
reserved
rhabdoid
rights
screened
sense
snf
subunits
swi
trisomy
truncating
|
|
Tagcloud (Difference) ? |
abnormality
arid1a
coinactivation
copyright
fish
frame
harboring
heterozygous
infancy
insights
malignancies
missense
monoploid
mrts
pbrm1
protected
remodeling
reserved
rhabdoid
rights
screened
sense
snf
subunits
swi
trisomy
truncating
|
|
Tagcloud (Intersection) ? |
|